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NCT00292539 Clinical Trial

Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class

Atrial Fibrillation Clinical Trial

Official title:
Preserve Registry: Prospective Registry of Pacemaker Patients Concerning Percentage of Right Ventricular Pacing, LVEF and NYHA Class

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00292539
Other study ID # Preserve Registry
Secondary ID
Status Completed
Phase N/A
First received February 14, 2006
Last updated April 22, 2009
Start date February 2006
Est. completion date September 2006

Study information
Verified date April 2009
Source Guidant Corporation
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

This registry is a data collection on patients who are implanted for more than 6 months with a pacemaker. Frequency and distribution of right ventricular pacing, NYHA class and left ventricular ejection fraction shall be documented.

Recruitment information / eligibility
Status Completed
Enrollment 600
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Implanted pacemaker for more than 6 months, VVI/DDD, written consent

Exclusion Criteria:

- Pacemaker implanted for less than 6 months, no right ventricular pacing possibility (AAI), no consent

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Device:
• Any pacemaker with right ventricular pacing option

Locations
Country Name City State
Germany Kreiskrankenhaus Viechtach

Sponsors (1)
Lead Sponsor Collaborator
Guidant Corporation

Country where clinical trial is conducted

Germany, 

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